# Sumatriptan

NDC: 68071-3525
Generic name: Sumatriptan
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220218

FDA application: ANDA078284

## Active ingredients

- SUMATRIPTAN SUCCINATE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-3525"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3525
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=082d05f6-3850-0fa2-e063-6294a90a0c66